A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514442



Internal ID22572400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81949158..81951200hg38UCSC Ensembl
chr9:84564073..84566115hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg382043
hg192043
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856088
Supporting Variants
Samples
Known GenesSPATA31D3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514442
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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